Foster C A, Holbrook K A, Farr A G
J Invest Dermatol. 1986 Mar;86(3):240-3. doi: 10.1111/1523-1747.ep12285201.
Langerhans cells (LCs) have been identified in human skin by 10 weeks estimated gestational age (EGA), but it was not known when they first enter the epidermis or acquire HLA-DR, OKT-6, and ATPase reactivity. We assayed for LCs in human embryonic and fetal skin by using immunolabeling and histochemical techniques on epidermal sheets. HLA-DR+ and ATPase+ LCs were present in the epidermis by 6-7 weeks EGA, the youngest tissue examined. Most LCs were OKT-6- until about 12 weeks EGA when they underwent a dramatic increase in OKT-6 reactivity. Although LC densities between 50-100 days were statistically similar (100 cells/mm2 of epidermis), LCs early in development were smaller, less dendritic, and phenotypically heterogeneous. We conclude that LCs migrate into the epidermis during the first trimester and resemble the adult phenotype by the second trimester, long before the immune system is fully activated.
在估计孕龄(EGA)为10周时,人类皮肤中已鉴定出朗格汉斯细胞(LCs),但尚不清楚它们何时首次进入表皮或获得HLA-DR、OKT-6和ATP酶反应性。我们通过对表皮片使用免疫标记和组织化学技术,检测了人类胚胎和胎儿皮肤中的LCs。在检测的最早期组织即EGA为6 - 7周时,表皮中就已存在HLA-DR+和ATP酶+的LCs。大多数LCs在大约EGA为12周之前呈OKT-6阴性,之后OKT-6反应性急剧增加。尽管50 - 100天时的LC密度在统计学上相似(每平方毫米表皮100个细胞),但发育早期的LCs较小,树突较少,且表型异质性较高。我们得出结论,LCs在妊娠前三个月迁移到表皮,并在妊娠中期免疫系统完全激活之前很久就类似于成年表型。